chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10567304	10567305	G	C	32	GENIC	homozygous	110954352
17	10567961	10567962	G	A	42	GENIC	homozygous	110954354
17	10569857	10569858	T	C	31	GENIC	homozygous	110954356
17	10570724	10570725	G	A	47	GENIC	homozygous	110954358
17	10572251	10572252	A	G	34	GENIC	homozygous	110954360
17	10572288	10572289	C	G	28	GENIC	possibly homozygous	110954362
17	10572381	10572382	C	T	28	GENIC	possibly homozygous	110954364
17	10572435	10572436	C	T	37	GENIC	possibly homozygous	110954366
17	10572641	10572642	T	C	51	GENIC	homozygous	110954368
17	10572858	10572859	A	T	33	GENIC	homozygous	110954370
17	10573122	10573123	G	T	25	GENIC	homozygous	110954372
17	10573639	10573640	G	A	37	GENIC	homozygous	110954374
17	10574326	10574327	G	A	31	GENIC	homozygous	111231018
17	10574463	10574464	A	G	57	GENIC	heterozygous	119263984